Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3295
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dc.contributor.authorKumar, Rohit-
dc.contributor.authorYadav, Sukrampal-
dc.contributor.authorPatil, Sunil A.-
dc.date.accessioned2020-12-22T05:04:48Z-
dc.date.available2020-12-22T05:04:48Z-
dc.date.issued2020-
dc.identifier.citationJournal of Hazardous, Toxic, and Radioactive Waste, 24(4)en_US
dc.identifier.other10.1061/(ASCE)HZ.2153-5515.0000533-
dc.identifier.urihttps://ascelibrary.org/doi/10.1061/%28ASCE%29HZ.2153-5515.0000533-
dc.identifier.urihttp://hdl.handle.net/123456789/3295-
dc.description.abstractThe removal of heavy metals from contaminated waters is highly desirable to circumvent their toxic effects on the ecosystem and human health. In this study, we report on the bioanode-assisted removal of mercury (Hg2+) at the cathode of microbial fuel cells (MFCs). An anode with an acetate-grown microbial electroactive biofilm, referred to as a bioanode, was used to facilitate the reduction of Hg2+ ions at the cathode of two-chambered MFCs. The MFCs with only Hg2+ as an electron acceptor achieved an open-circuit voltage of 778 ± 18.4 mV and a power density of 32.6 ± 0.5 mW/m2. Up to 98% Hg2+ removal efficiency at a rate of 0.4 mg/L/h, from an initial 10 mg/L to the final 0.2 mg/L Hg2+ concentration in the catholyte, was achieved in 24-h tests. Inductively-coupled plasma mass spectrometry analysis revealed deposition of up to 8.84 mg/L of Hg at the cathode surface. Even a low Hg2+ concentration of 0.270 mg/L was removed efficiently at a rate of 0.19 mg/L/h by the MFCs. The cathode potential changed according to the concentration or availability of Hg2+ in the catholyte.en_US
dc.language.isoen_USen_US
dc.publisherAmerican Society of Civil Engineersen_US
dc.subjectBioelectrochemical systemsen_US
dc.subjectElectrode-assisted bioremediationen_US
dc.subjectMercury removalen_US
dc.subjectMicrobial electroactive biofilmen_US
dc.titleBioanode-Assisted Removal of Hg2+ at the Cathode of Microbial Fuel Cellsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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